Clinical Supplies Specialist
4 weeks ago
About the Role
We are seeking a skilled Clinical Supplies Specialist to join our team at Novo Nordisk. As a Clinical Supplies Specialist, you will play a critical role in ensuring the smooth execution of clinical trials.
Main Responsibilities
- Ensure clinical supply input to clinical trial protocols
- Create trial master data, clinical label text, and trial-specific manuals to be used by clinical sites and aligned with product specifications and regulatory requirements
- Ensure documents are ready for clinical trial application to authorities
Requirements
- MSc degree in Natural, Health, or Pharmaceutical Sciences or similar
- Experience in the pharma industry will be a plus
- Quality mindset and experience with regulatory requirements, e.g., GCP and GMP
- Data-driven, analytical, and methodical capabilities with flair for IT systems and tools
- Excellent collaboration and communication skills with fluency in English
About the Department
The Clinical Supplies Trial Set-up department consists of six teams who prepare clinical trials for supply execution by forecasting product demand, simulating trial supply execution, setting up supply systems, and preparing regulatory documents for CTA.
Working at Novo Nordisk
We don't wait for change. We drive it. We're a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing, and sales – we're all working to move the needle on patient care.
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